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Asymmetric paired oxidative and reductive catalysis enables enantioselective alkylarylation of olefins with C(sp<sup>3</sup>)−H bonds.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-52248-y
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- Article
Asymmetric paired oxidative and reductive catalysis enables enantioselective alkylarylation of olefins with C(sp<sup>3</sup>)−H bonds.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-52248-y
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- Publication type:
- Article
Nickel‐Catalyzed Cross‐Coupling of Sulfonamides With (Hetero)aryl Chlorides.
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- Angewandte Chemie, 2020, v. 132, n. 23, p. 9037, doi. 10.1002/ange.202002392
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- Article
Berichtigung: Palladium(I) Dimer Enabled Extremely Rapid and Chemoselective Alkylation of Aryl Bromides over Triflates and Chlorides in Air.
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- Angewandte Chemie, 2020, v. 132, n. 20, p. 7715, doi. 10.1002/ange.202002528
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- Article
Sulfur(IV)‐Mediated Unsymmetrical Heterocycle Cross‐Couplings.
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- Angewandte Chemie, 2020, v. 132, n. 19, p. 7442, doi. 10.1002/ange.201915425
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- Article
Copper‐Catalyzed Enantioselective Allylic Alkylation with a γ‐Butyrolactone‐Derived Silyl Ketene Acetal.
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- Angewandte Chemie, 2020, v. 132, n. 5, p. 2049, doi. 10.1002/ange.201912618
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- Article
Palladium–Borane Cooperation: Evidence for an Anionic Pathway and Its Application to Catalytic Hydro‐/Deutero‐dechlorination.
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- Angewandte Chemie, 2019, v. 131, n. 52, p. 18959, doi. 10.1002/ange.201909675
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- Article
Visible‐Light‐Promoted Iron‐Catalyzed C(sp<sup>2</sup>)–C(sp<sup>3</sup>) Kumada Cross‐Coupling in Flow.
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- Angewandte Chemie, 2019, v. 131, n. 37, p. 13164, doi. 10.1002/ange.201906462
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- Article
Synthesis and Reactivity of Paramagnetic Nickel Polypyridyl Complexes Relevant to C(sp<sup>2</sup>)–C(sp<sup>3</sup>)Coupling Reactions.
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- Angewandte Chemie, 2019, v. 131, n. 18, p. 6155, doi. 10.1002/ange.201901866
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- Article
Efficient Electrocatalysis for the Preparation of (Hetero)aryl Chlorides and Vinyl Chloride with 1,2‐Dichloroethane.
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- Angewandte Chemie, 2019, v. 131, n. 14, p. 4614, doi. 10.1002/ange.201814570
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- Article
Palladium‐Catalyzed Construction of Quaternary Stereocenters by Enantioselective Arylation of γ‐Lactams with Aryl Chlorides and Bromides.
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- Angewandte Chemie, 2019, v. 131, n. 13, p. 4341, doi. 10.1002/ange.201814475
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- Article
Photoinduced Miyaura Borylation by a Rare‐Earth‐Metal Photoreductant: The Hexachlorocerate(III) Anion.
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- Angewandte Chemie, 2018, v. 130, n. 34, p. 11165, doi. 10.1002/ange.201804022
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- Article
Cobalt-Catalyzed Suzuki Biaryl Coupling of Aryl Halides.
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- Angewandte Chemie, 2017, v. 129, n. 51, p. 16585, doi. 10.1002/ange.201710053
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- Article
Nickel-Catalyzed Cyanation of Aryl Chlorides and Triflates Using Butyronitrile: Merging Retro-hydrocyanation with Cross-Coupling.
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- Angewandte Chemie, 2017, v. 129, n. 49, p. 15899, doi. 10.1002/ange.201707517
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- Article
Mild, Redox-Neutral Formylation of Aryl Chlorides through the Photocatalytic Generation of Chlorine Radicals.
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- Angewandte Chemie, 2017, v. 129, n. 25, p. 7297, doi. 10.1002/ange.201702079
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- Article
Room-Temperature Arylation of Thiols: Breakthrough with Aryl Chlorides.
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- Angewandte Chemie, 2017, v. 129, n. 3, p. 892, doi. 10.1002/ange.201610414
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- Article
ortho-C−H Arylation of Benzoic Acids with Aryl Bromides and Chlorides Catalyzed by Ruthenium.
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- Angewandte Chemie, 2016, v. 128, n. 47, p. 14972, doi. 10.1002/ange.201607270
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- Article
Nickel-Catalyzed Monoarylation of Ammonia.
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- Angewandte Chemie, 2015, v. 127, n. 12, p. 3844, doi. 10.1002/ange.201410875
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- Article
Nickel-Catalyzed Amination of Aryl Chlorides with Ammonia or Ammonium Salts.
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- Angewandte Chemie, 2015, v. 127, n. 12, p. 3839, doi. 10.1002/ange.201500404
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- Article
Synergistic Steric Effects in the Development of a Palladium-Catalyzed Alkyne Carbohalogenation: Stereodivergent Synthesis of Vinyl Halides.
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- Angewandte Chemie, 2015, v. 127, n. 1, p. 256, doi. 10.1002/ange.201409248
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- Article
Continuous flow aminolysis under high temperature and pressure.
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- Journal of Flow Chemistry, 2020, v. 10, n. 1, p. 145, doi. 10.1007/s41981-019-00049-6
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- Article
Mercuration and Telluration of 2-Fluoro-5-nitroaniline: Synthesis, Antibacterial, and Computational Study.
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- Russian Journal of General Chemistry, 2020, v. 90, n. 4, p. 703, doi. 10.1134/S1070363220040222
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- Article
LiCl-Accelerated Nickel Catalyzed Cross-Coupling of Aryl Tosylates with the Aryl Grignard Reagents.
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- Russian Journal of General Chemistry, 2019, v. 89, n. 12, p. 2591, doi. 10.1134/S1070363219120405
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- Article
Reactions of Benzylidene Chlorides with S-Methyl Diethylphosphinothioate.
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- Russian Journal of General Chemistry, 2019, v. 89, n. 12, p. 2386, doi. 10.1134/S1070363219120107
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- Publication type:
- Article
Unexpected Effect of N-Heterocyclic Carbene on the Catalytic Activity of Palladium Complex in the Cross-Coupling Reaction of K[C<sub>6</sub>F<sub>5</sub>BF<sub>3</sub>] with Aryl Chlorides.
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- Doklady Chemistry, 2023, v. 513, n. 1, p. 337, doi. 10.1134/S0012500823600979
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- Article
High-performance heterogeneous catalysis with surface-exposed stable metal nanoparticles.
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- Scientific Reports, 2014, p. 1, doi. 10.1038/srep07228
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- Article
Preformed Pd(II) Catalysts Based on Monoanionic [N,O] Ligands for Suzuki-Miyaura Cross-Coupling at Low Temperature.
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- Catalysts (2073-4344), 2023, v. 13, n. 2, p. 303, doi. 10.3390/catal13020303
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- Article
Synthesis of Xylyl-Linked Bis-Benzimidazolium Salts and Their Application in the Palladium-Catalyzed Suzuki–Miyaura Cross-Coupling Reaction of Aryl Chlorides.
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- Catalysts (2073-4344), 2021, v. 11, n. 7, p. 817, doi. 10.3390/catal11070817
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- Article
Ni-Containing Catalysts.
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- 2021
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- Editorial
Editorial Catalysts : Special Issue on Transition Metal Catalyzed Cross-Coupling Reactions.
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- 2021
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- Editorial
Synthesis of Alkynyl Ketones by Sonogashira Cross-Coupling of Acyl Chlorides with Terminal Alkynes Mediated by Palladium Catalysts Deposited over Donor-Functionalized Silica Gel.
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- Catalysts (2073-4344), 2020, v. 10, n. 10, p. 1186, doi. 10.3390/catal10101186
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- Article
Palladium PEPPSI-IPr Complex Supported on a Calix[8]arene: A New Catalyst for Efficient Suzuki–Miyaura Coupling of Aryl Chlorides.
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- Catalysts (2073-4344), 2020, v. 10, n. 9, p. 1081, doi. 10.3390/catal10091081
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- Article
Catalysts for Suzuki–Miyaura Coupling Reaction.
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- 2020
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- Publication type:
- Editorial
Development of Titanium Dioxide-Supported Pd Catalysts for Ligand-Free Suzuki–Miyaura Coupling of Aryl Chlorides.
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- Catalysts (2073-4344), 2019, v. 9, n. 5, p. 461, doi. 10.3390/catal9050461
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- Article
Synthesis of the First Resorcin[4]arene-Functionalized Triazolium Salts and Their Use in Suzuki–Miyaura Cross-Coupling Reactions.
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- Catalysts (2073-4344), 2019, v. 9, n. 4, p. 388, doi. 10.3390/catal9040388
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- Article
A Tuned Bicyclic Proazaphosphatrane for Catalytically Enhanced N-Arylation Reactions with Aryl Chlorides.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 9, p. 1954, doi. 10.1002/ejoc.201403428
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- Article
The Suzuki-Miyaura Reaction Performed Using a Palladium-N-Heterocyclic Carbene Catalyst and a Weak Inorganic Base.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 9, p. 1920, doi. 10.1002/ejoc.201500043
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- Article
A Versatile and Efficient Palladium- meta-Terarylphosphine Catalyst for the Copper-Free Sonogashira Coupling of (Hetero-)Aryl Chlorides and Alkynes.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 32, p. 7184, doi. 10.1002/ejoc.201402699
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- Article
Suzuki-Miyaura Coupling of Aryl Chlorides with Arylboronic Acids Using the Morpholine-NiCl<sub>2</sub> Catalyst System.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 31, p. 6983, doi. 10.1002/ejoc.201402881
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- Publication type:
- Article
Synergistic Effect of a Bis(proazaphosphatrane) in Mild Palladium-Catalyzed Direct α-Arylations of Nitriles with Aryl Chlorides.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 27, p. 6025, doi. 10.1002/ejoc.201402466
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- Article
Tröger's Base Derived Phosphanes for Suzuki-Miyaura and Buchwald-Hartwig Cross-Coupling Reactions.
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- European Journal of Organic Chemistry, 2013, v. 2013, n. 20, p. 4233, doi. 10.1002/ejoc.201300519
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- Article
Application of Biaryl Phosphacycles in Palladium‐Catalysed Suzuki‐Miyaura Cross‐Coupling Reactions of Aryl Chlorides.
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- European Journal of Inorganic Chemistry, 2024, v. 27, n. 17, p. 1, doi. 10.1002/ejic.202400068
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- Article
General and Mild Ni<sup>0</sup>-Catalyzed α-Arylation of Ketones Using Aryl Chlorides.
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- Chemistry - A European Journal, 2015, v. 21, n. 10, p. 3906, doi. 10.1002/chem.201406457
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- Article
Borylation of Unactivated Aryl Chlorides under Mild Conditions by Using Diisopropylaminoborane as a Borylating Reagent.
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- Chemistry - A European Journal, 2014, v. 20, n. 19, p. 5573, doi. 10.1002/chem.201304861
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- Article
BippyPhos: A Single Ligand With Unprecedented Scope in the Buchwald-Hartwig Amination of (Hetero)aryl Chlorides.
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- Chemistry - A European Journal, 2013, v. 19, n. 49, p. 16760, doi. 10.1002/chem.201302453
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- Article
Unveiling the potential of Pd(II)‐covalent organic polyimide framework in Suzuki coupling reactions: A study on synthesis, characterization, and catalytic efficiency.
- Published in:
- Applied Organometallic Chemistry, 2024, v. 38, n. 2, p. 1, doi. 10.1002/aoc.7333
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- Article
A sustainable approach for efficient one‐pot synthesis of 1‐aryl 1,2,3‐triazoles using copper iodide supported on 3‐thionicotinyl‐urea‐modified magnetic nanoparticles in DES.
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- Applied Organometallic Chemistry, 2021, v. 35, n. 7, p. 1, doi. 10.1002/aoc.6255
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- Article
Bimetallic Pd<sub>x</sub>Ni<sub>1‐x</sub> and Pd<sub>x</sub>Co<sub>1‐x</sub> nanoparticles supported on K‐OMS‐2: Highly active, environmentally friendly and reusable nanocatalysts for the Suzuki–Miyaura cross‐coupling reactions in water
- Published in:
- Applied Organometallic Chemistry, 2021, v. 35, n. 2, p. 1, doi. 10.1002/aoc.6096
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- Article
A new Pd(II)‐supported catalyst on magnetic SBA‐15 for CC bond formation via the Heck and Hiyama cross‐coupling reactions.
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- Applied Organometallic Chemistry, 2021, v. 35, n. 2, p. 1, doi. 10.1002/aoc.6078
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- Article
Markovnikov versus anti‐Markovnikov addition and C–H activation: Pd–Cu synergistic catalysis.
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- Applied Organometallic Chemistry, 2021, v. 35, n. 1, p. 1, doi. 10.1002/aoc.6077
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- Article